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HRID 2392879作成日:2026年10月25日

Methanol → 4-(3,4-Dihydroxybenzyl)amino-6,7,8-trimethoxyquinazoline hydrochloride

https://huagongshe.com/reaction/2392879

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Boron TrichlorideHCID 25135—
反応物4-((3,4-(Methylenedioxy)benzyl)amino)-6,7,8-trimethoxyquinazolineHCID 205964—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物4-(3,4-Dihydroxybenzyl)amino-6,7,8-trimethoxyquinazoline hydrochlorideHCID 18796743—

反応手順

30 ml of a 1.0M solution of boron trichloride in methylene chloride was dropped into a solution of 2.00 g (5.41 mmol) of 4-(3,4-methylenedioxybenzyl)amino-6,7,8-trimethoxyquinazoline in 150 ml of chloroform under stirring at room temperature. The obtained mixture was stirred at room temperature for 2 days, followed by the addition of methanol and the obtained mixture was distilled under a reduced pressure to remove the solvent. This procedure was repeated thrice and the obtained residue was purified by silica gel column chromatography (chloroform/n-hexane). Hydrochloric acid/ethanol was added to the eluate and the obtained mixture was distilled under a reduced pressure to remove the solvent, followed by the addition of ethanol. The crystals thus formed were recovered by filtration. Thus, 0.59 g of the title compound was obtained as a colorless needle.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05801180
出典データセットuspto-grants-1998_09
ORD IDord-12143d897a70401f91ec62f46008b76d
出典メモuspto-grants-1998_09